Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/0005—Other compounding ingredients characterised by their effect
  • C11D3/0026—Low foaming or foam regulating compositions
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D19/00—Degasification of liquids
  • B01D19/02—Foam dispersion or prevention
  • B01D19/04—Foam dispersion or prevention by addition of chemical substances
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D19/00—Degasification of liquids
  • B01D19/02—Foam dispersion or prevention
  • B01D19/04—Foam dispersion or prevention by addition of chemical substances
  • B01D19/0404—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
  • B01D19/0409—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing Si-atoms
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
  • C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers
  • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers
  • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
  • C11D3/3738—Alkoxylated silicones
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers
  • C11D3/3788—Graft polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
  • C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure

Definitions

• the disclosure provides a defoaming agent for a liquid detergent, having a strong foam control effect, capable of ensuring clarity of detergents, and belonging to the technical field of fine chemical.
• liquid detergents As daily necessities for people, liquid detergents have become prevailing detergents because they are simple in process equipment, are easy to use, are fast dissolving, are milder for fabric and skin, etc. Due to high content and much foam, surfactants are difficult to rinse, not only waste water resources, and increase the washing cost, but also will result in large-scale water pollution, and go against energy conservation, emission reduction and environmental protection.
• defoaming agents can quickly penetrate into the foam system, resulting in the bubble burst.
• the defoaming agent can effectively solve the problem of much foam and difficult rinse in the washing process.
• the defoaming agents used in detergents are mainly organosilicone defoaming agents.
• compatibility and clarity have always been very important knotty problems, especially clarity.
• a detergent will become turbid, and fail to reach aesthetic requirements.
• Polydimethylsiloxane has relatively small surface tension. But due to relatively poor compatibility with organics, there is weak affinity between the active components of a defoaming agent and a foam film, thereby resulting in poor defoaming performance.
• DE-A2025722 discloses to disperse hydrophobic silica in polydimethylsiloxane, but the obtained defoaming agent has a poor defoaming performance.
• DE-B2222998 selects to introduce a polyether group into polydimethylsiloxane. The introduction of the polyether group solves the compatibility problem, but the defoaming efficiency is low, thereby increasing the use cost.
• the hydrophobic performance is improved, but the compatibility with organics is significantly improved, and the affinity between defoaming particles and a foam film is enhanced, thereby contributing to defoaming.
• EP1075684 discloses a foam control agent for a liquid detergent, comprising an organic-based polysiloxane material, an organosilicon resin and a hydrophobic filler, wherein the organopolysiloxane material comprises organopolysiloxane having at least one silicon-bonded substituent having the molecular formula X-Ar, wherein X represents a divalent aliphatic group bonded to silicon through a carbon atom, and Ar represents an aromatic group.
• Organic-based resin is selected from the group consisting of siloxane units having the formula RaSiO (4-a)/2 , wherein R represents a hydroxyl group, a hydrocarbon or ahydrocarbonoxy group and a has an average value from 0.5 to 2.4.
• EP1075683 discloses a foam inhibitor with similar composition, except that it contains a water-insoluble organic liquid, which may be a mineral oil, a liquid polyisobutene or a vegetable oil.
• CN102307978A also discloses a foam inhibitor with similar composition, comprising, on the basis of EP1075684 , an organopolysiloxane resin having at least one polyoxyalkylene group, wherein the organopolysiloxane resin comprises tetrafunctionalsiloxane units having the formula RSiO 4/2 and monofunctionalsiloxane units having the formula R 3 SiO 4/2 .
• the total number of tetrafunctionalsiloxane units in the resin is at least 50% based on the total number of siloxane units, and R represents a hydroxyl group.
• This liquid foam inhibitor is used in heavy duty liquid (HDL) detergents to solve the stability and foam control performance of the composition in detergents, but the turbidity of liquid detergents is increased in appearance.
• HDL heavy duty liquid
• Polyorganosiloxane is modified with an alkyl group to improve the binding force between the organosilicone defoaming composition and organic materials, so that the synthetic organosilicon emulsion has excellent defoaming performance in anionic and non-ionic systems.
• EPA578424 discloses a foam inhibitor comprising a polydimethylsiloxane with an alkyl side chain, wherein the alkyl side chain contains 9 to 35 carbon atoms, and 40 to 100% silicone composition carries a hydroxyl group having 9 to 35 carbon atoms.
• EPA121210 discloses a modified phlysiloxane having an alkyl group having 6 to 30 carbon atoms, provided that the number of carbon atoms accounts for 30 to 65% in the group "-CH2-", in order to obtain an efficient defoaming agent in combination with a mineral oil.
• CN102698475A introduces a defoaming composition, which is characterized by being prepared by the following steps of: obtaining an alkyl-modified polyorganosilicone through reaction of a hydrogen-containing polyorganosilicone, an ⁇ -olefin and a vinyl polyorganosilicone; and adding silica, an organic silicon resin and an aminopolyorganosilicone, mixing same so as to obtain an organosilicone defoaming composition, which can be used for a defoaming component in organosilicone emulsions and solid defoaming agents.
• a solid particle defoaming agent prepared by using the obtained active component has a sustained release effect and a foam control effect.
• CN103272411A relates to a foam inhibitor and a preparation process thereof.
• the preparation process comprises: obtaining a polyorganosiloxane modified by an alkyl and an unsaturated polyether through reaction of a hydrogen-containing polyorganosiloxane, an unsaturated polyether and an ⁇ -olefin in the presence of an acid catalyst; and then adding a hydrophobic particle and an organosilicon resin, mixing same, preparing an O/W emulsion of defoaming agent through emulsification of the active component of the obtained foam inhibitor, and adding the O/W emulsion of the defoaming agent to a non-structural detergent.
• the foam inhibitor can solve the clarity and attenuation of defoaming properties, but will still have the problem of defoaming agent precipitation after prolonged storage.
• CN102307978A discloses an organopolysiloxane polymer, the preparation of which comprises: preparing a crosslinked siloxane polymer through reaction of a linear hydrogen-containing polyorganosiloxane and bivinylpolysiloxane in the presence of a catalyst, and then introducing a polyoxyalkylenesiloxane into the crosslinked polymer to obtain a crosslinked siloxane polymer with side chains.
• a defoaming composition prepared from the polymer and an organic-based siloxane material containing X-Ar is used in a detergent to have better defoaming properties. But its stability in the detergent is not disclosed.
• These polymers are described in, for example, EP0663225 , CN1331278 and EP1167502B1 .
• the emulsifier used in preparing an O/W emulsion from an organosilicon composition must have strong affinity with the composition, and can form a stable monomolecular film on the surface of oil drops.
• an organosilicon composition with alkyl groups due to the presence of alkyl groups, ordinary siloxane polymer containing a polyoxyalkylenesiloxane is less compatible with the siloxane composition.
• a single emulsifier cannot reach the effect of compounding a plurality of emulsifiers.
• the present invention compounds a branched siloxane polymer modified by an alkyl and a polyether with a crosslinked modified siloxane polymer prepared from an unsaturated polyether, a bivinyl-terminated polyorganosiloxane and a hydrogen-containing polyorganosiloxane, so as to reach a better emulsification and dispersion effect for organosilicon compositions having alkyl groups.
• the compatibility and synergistic effect between both and other components enable the prepared defoaming agent emulsion to have excellent defoaming performance and clarity in a liquid detergent, and also have excellent stability, so as to ensure that the defoaming agent neither precipitates, nor aggregates in a laundry detergent, and effectively solve the phenomena, such as coagulation and aggregation.
• the objective of the present invention can be achieved through the following measures:
• the defoaming agent for a liquid detergent referred to in the present invention can be formed by mixing the above components only, can further include other components, such as a pH regulating agent or a catalyst existing in the components, and can be further added with other components without bad effects on the overall performance of the present invention to further improve the performance in an aspect or some aspects, for example, the defoaming agent further includes a component E: 1-10 parts by weight of an emulsifier, or can further include a component F: 0.01-0.5 parts by weight of a preservative.
• the present invention can also further only include any one or a combination of two of the component E and component F.
• the use level and mixing ratio are: component A1: 4-15 parts by weight, component A2: 5-20 parts by weight, component B: 5-15 parts by weight, component C: 0.5-5 parts by weight, component D: 60-80 parts by weight, and component E: 1-10 parts by weight.
• the use level and mixing ratio are: component A1: 4-10 parts by weight, component A2: 5-18 parts by weight, component B: 8-15 parts by weight, component C: 0.5-5 parts by weight, component D: 60-80 parts by weight, and component E: 1-10 parts by weight.
• the components of the present invention can be prepared by using existing process.
• the raw material of component B organosilicon composition contains the components that are not used in the prior art, but can still be prepared using existing process.
• a component A1 modified polyorganosiloxane is obtained through reaction of a hydrogen-containing polyorganosiloxane, an unsaturated polyether and an ⁇ -olefin in the presence of a catalyst at 80-180°C.
• a component A2 modified polyorganosiloxane is obtained through reaction of a hydrogen-containing polyorganosiloxane, an unsaturated polyether and a bivinyl-terminated polyorganosiloxane in the presence of a catalyst at 80-180°C.
• component B is as follows: firstly a hydrogen-containing polyorganosiloxane is fully mixed with an acrylate, to which a catalyst is added at 60-80°C. Then, after the system is heated to 90-110°C and kept at the temperature, an ⁇ -olefin is added thereto, and further kept at the temperature. Finally, silica and an organosilicon resin are added and mixed to obtain the component B.
• the modified polyorganosiloxane is obtained through reaction of a modifying group and a hydrogen-containing polyorganosiloxane in the presence of a catalyst.
• the modifying group is two or three selected from the group consisting of an unsaturated polyether, an ⁇ -olefin and a bivinyl-terminated polyorganosiloxane.
• the average viscosity of the modified polyorganosiloxane at 25°C is 10-30,000 mPa• S, preferably 100-3,000 mPa• s.
• a hydrogen-containing polyorganosiloxane at least has a general structural formula as follows: H c Me 3 - c SiO(MeHSiO) a (Me 2 SiO) b SiMe 3 - c H c Me is a methyl group, the subscript c is 0 or 1, and a is an integer from 2 to 100, preferably an integer from 10 to 70. b is an integer from 20 to 300, preferably an integer from 40 to 200. Each molecule has at least 2 silicon-bonded hydrogen atoms.
• the dynamic viscosity of the hydrogen-containing polyorganosiloxane at 25°C is 20-5,000 mPa• s. In a solution, there are 40-80 parts by weight of a hydrogen-containing polyorganosiloxane in the modified polyorganosiloxane.
• the unsaturated polyether has the general structure formula as follows: ViCH 2 O(EO) x (PO)yR 1 Vi is a vinyl, R 1 is selected from hydrogen, alkyl group having 1 to 6 carbon atoms, ester group, epoxy group or amino group; EO is ethylene oxide, PO is propylene oxide, x and y are degrees of polymerization, x is an integer from 0 to 150, preferably from 0 to 40; and y is an integer from 0 to 150, preferably from 0 to 100. x and y cannot both be 0. In a solution, there are 20-40 parts by weight of an unsaturated polyether in the modified polyorganosiloxane.
• the ⁇ -olefin has the general structural formula as follows: Vi(CH 2 ) z H Vi is a vinyl, and z is an integer from 1 to 36, preferably an integer from 6 to 18. In a solution, there are 10-30 parts by weight of an ⁇ -olefin in the modified polyorganosiloxane.
• the bivinyl-terminated polyorganosilicone has the general structural formula as follows: Vi(R 2 ) 2 SiO((R 2 ) 2 SiO) m Si(R 2 ) 2 Vi m is an integer from 100 to 500, preferably from 200 to 400; R 2 is an alkyl group having 1-6 carbon atoms, preferably a methyl group.
• the dynamic viscosity of the bivinyl-terminated polyorganosiloxane at 25°C is 50-2,000 mPa• s. In a solution, there are 10-30 parts by weight of a bivinyl-terminated polyorganosiloxane in the modified polyorganosiloxane.
• the catalyst is one selected from the group consisting of platinum-alcohol complex, platinum-olefin complex, platinum-alkoxide complex, platinum-ether complex, platinum-ketone complex, isopropanol solution of chloroplatinic acid or platinum-vinyl complex.
• the catalyst in this process is preferably an isopropanol solution of chloroplatinic acid with the platinum content of 1-20ppm.
• the mass ratio of a catalyst in the modified polyorganosiloxane is 0.01-0.2%.
• Component A1 The modified polyorganosiloxane A1 is obtained through reaction of the above hydrogen-containing polyorganosiloxane A (I), unsaturated polyether A (II), and ⁇ -olefin A (III), as well as a catalyst A (V), in a reactor at 80-180°C for 0.5-3hours.
• Component A2 The modified polyorganosiloxane A2 is obtained through reaction of the above hydrogen-containing polyorganosiloxane A (I), unsaturated polyether A (II), and bivinyl-terminated polyorganosilicone A (IV), as well as a catalyst A (V), in a reactor at 80-180°C for 0.5-3hours.
• the organoilicone composition according to the present invention is prepared from a hydrogen-containing polyorganosiloxane, an acrylate, a catalyst, an ⁇ -olefin, silica, and an MQ resin using a prior art known to those skilled in the art.
• a solution there are 2-20 parts by weight of an organoilicone composition in a defoaming agent, preferably 5-20 parts by weight, more preferably 8-15 parts by weight.
• the range of choice of the hydrogen-containing polyorganosiloxane is the same as above, i.e. A(I).
• A(I) the range of choice of the hydrogen-containing polyorganosiloxane
• the range of choice of the catalyst is the same as above, i.e. A(V), preferably an isopropanol solution of chloroplatinic acid with the platinum content of 1-20ppm.
• A(V) preferably an isopropanol solution of chloroplatinic acid with the platinum content of 1-20ppm.
• the mass ratio of a catalyst in an organosilicon composition is 0.01-0.2%.
• the range of choice of the ⁇ -olefin is the same as above, i.e. A(III).
• A(III) the range of choice of the ⁇ -olefin.
• the silica includes hydrophobized or non-hydrophobizedfumed silica or precipitated silica having a specific surface area of 50-500 m 2 /g.
• the precipitated silica or fumed silica having a specific surface area of 90-300 m 2 /g is preferable in the present invention.
• the organosilicon resin refers to a highly cross-linked polyorganosiloxane having a spatial mesh structure
• the polyorganosiloxane having a spatial mesh structure is usually obtained through obtaining an acidic hydrolysate by hydrolyzing various mixtures of methyltrichlorosilane, dimethyldichlorosilane, phenyltrichlorosilane, diphenyldichlorosilane and methylphenyldichlorosilane in an organic solvent, such as toluene, and then removing acid by washing with water.
• the organosilicon resin used in the present invention is an MQ resin composed of chain units CH 3 SiO 1/2 (called M units in organosilicone chemistry) and chain units SiO 4/2 (Q units), and the molar ratio between the two is (0.4-1.2): 1.0, preferably (0.5-0.8): 1.0.
• M units chain units CH 3 SiO 1/2
• Q units chain units SiO 4/2
• molar ratio between the two is (0.4-1.2): 1.0, preferably (0.5-0.8): 1.0.
• the acrylate is esters of acrylic acid and its homologue, including methyl acrylate, ethyl acrylate, butyl acrylate, isobutyl acrylate, 2-methyl methacrylate, 2-ethyl methacrylate and 2-butyl methacrylate.
• a solution there are 3-15 parts by weight of an acrylate in an organoilicone composition.
• a specific preparation process of an organoilicone composition B is as follows: firstly the above hydrogen-containing polyorganosiloxane is fully mixed with an acrylate, to which a catalyst is added at 70°C. Then, after the system is heated to 100°C and kept at the temperature for 1 hour, an ⁇ -olefin is added thereto, and further kept at the temperature for 2 hours. Finally, silica and an organosilicon resin are added and mixed to obtain the organoilicone composition B.
• the thickening agent is selected from the group consisting of polyacrylamide, carbomer, xanthan, cellulose and polyacrylic acid.
• Polyacrylic acid thickening agent is preferably used in the present invention to thicken the system by regulating the pH value using an alkali and controlling the viscosity of the system to 1000-5000mPa• s. In a solution, there are 0.5-5 parts by weight of a thickening agent in a defoaming agent.
• the water is deionized water. In a solution, there are 50-90 parts by weight of water in a defoaming agent. The mass content of water in a defoaming agent can be 50-90%.
• the emulsifier is an anionic, cationic or non-ionic surfactant, preferably a non-ionic surfactant.
• the non-ion surfactant is selected from the group consisting of polyoxyethylenenonylphenyl ether, polyoxyethyleneoctylphenol ether, polyoxyethylene lauryl ether, polyoxyethyleneoleyl ether, sorbitanmonstearate, sorbitanmonooleate, sorbitantristearate, sorbitantrioleate, polyoxyethylenesorbitanmonostearate, polyoxyethylenesorbitanmonooleate, polyoxyethylenesorbitantristearate, and polyoxyethylene castor oil.
• the emulsifiers may be used separately, or mixed before use.
• the preservative is one or more selected from the group consisting of methyl-p-hydroxybenzoate, ethyl-p-hydroxybenzoate, propyl-p-hydroxybenzoate, butyl-p-hydroxybenzoate, sodium diacetate, benzoic acid and sodium salt thereof, sorbic acid and potassium salt thereof, dimethyl fumarate, 2-methyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one, 4,5-dichloro-2-methyl-4-isothiazolin-3-one, 2-n-octyl-4-isothiazoline-3-one, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, 5-chloro-2-n-octyl-4-isothiazolin-3-one, 1,2-benzo-isothiazolin-3-one, n-nutyl-1,2-benzo-isothiazolin-3-one, and
• a defoaming agent can be prepared by controlling its pH value in an appropriate range according to an existing method, so as to facilitate preparation, production or use of the defoaming agent, wherein the pH range is generally 5.0-7.0, preferably 6.5-7.0.
• the pH value of defoaming can be regulated using an acid or alkali commonly used in this field.
• the defoaming agent of the present invention can be prepared using the following process: a modified polyorganosiloxane A1, a modified polyorganosiloxane A2 and an organosilicon composition B are mixed, heated to 50 -80°C, and fully stirred; then in the case of keeping a constant temperature while stirring, a part of a thickening agent and water are added, and the pH value is regulated to 6.5-7.0; finally, the emulsion thus obtained is homogenized, and the balance amount of the thickening agent and water are added.
• the amount of the first added thickening agent is 70-90% based on the total mass of the thickening agent, and the amount of the first added water is 30-60% based on the total mass of water.
• a defoaming agent of the present invention can be prepared specifically using a process comprising the following steps:
• an organosilicone defoaming agent of the present invention contains an emulsifier
• the emulsifier is generally mixed with A1 and A2 before addition.
• the preservative is finally added to the product.
• modified polyorganosiloxane A1 and A2 are compounded, and the compatibility and synergistic effect between the two and other components enable the obtained defoaming agent emulsion to have a good defoaming performance, clarity and excellent stability in a liquid detergent, so as to ensure that the defoaming agent neither precipitates, nor agglomerates in a laundry detergent, and effectively solve the phenomenon, such as coagulation and aggregation.
• modified polyorganosiloxane There are many other different combinations of modified polyorganosiloxane.
• the compounding effects are all worse than the compounding effect of the modified polyorganosiloxane A1 and A2 according to the present invention.
• Different combinations of modified polyorganosiloxane will exhibit different properties, which will be described specifically through examples and comparative examples.
• Table 1 Components A1-1 to A1-4, A2-5 to A2-8 and A-9 to A-14 of a modified polysiloxane Monomer A(I) A(II) A(III) A(IV) General formula/use level a b c Use level/g x y R 1 Use level/g z Use level/g m R 2 Use level/g A1-1 15 45 0 250 0 50 -CH 3 230 8 120 - - 0 A1-2 65 190 1 250 20 0 -H 120 16 230 - - 0 A1-3 100 170 1 300 35 90 -NH 3 200 12 100 - - 0 A1-4 30 150 0 450 30 70 -CH 3 90 16 60 - - 0 A2-5 15 45 0 250 0 50 -CH 3 250 - 0 210 -CH 3 100 A2-6 65 190 1 250 20 0 -H 230 - 0 390 -CH 3 120 A2-7 100
• Modified polysiloxane A1-1 to A1-4 are prepared through reaction of A (I), A (II) and A (III) after mixing them, A2-5 to A2-8 (i.e. A2-5, A2-6, A2-7 and A2-8) are prepared through reaction of A (I), A (II) and A (IV) after mixing them, A-9 to A-12 are prepared through reaction of A (I), A (II), A(III) and A (IV) after mixing them, and A-13 and A-14 are prepared through reaction of A (I) and A (II) after mixing them.
• each modified polysiloxane comprises first adding the above use level of A (I), A (II), A (III) and A (IV), as well as a catalyst A (V), in a reactor at 80-180°C for 0.5-3hours.
• the catalyst A (V) is an isopropanol solution of chloroplatinic acid with the platinum content of 5-15 ppm.
• the reaction temperature is 100-110°C, and the use level of the catalyst is 0.05-0.08% based on the mass of the modified polysiloxane.
• reaction temperature is 110-130°C, and the use level of the catalyst is 0.04-0.06% based on the mass of the modified polysiloxane.
• reaction temperature is 100-110°C, and the use level of the catalyst is 0.05-0.08% based on the mass of the modified polysiloxane.
• Organosilicon composition B1 was prepared as follows:
• Organosilicon composition B2 was prepared as follows:
• Organosilicon composition B3 was prepared as follows:
• Organosilicon composition B4 was prepared as follows:
• Organosilicon composition B5 was prepared as follows:
• Organosilicon composition B6 was prepared as follows:
• Example 1 Example Group Component A and use level Component B and use level Component C and use level Component D and use level Component E and use level Component F and use level Defoaming agent solid content
• Example 1 A1-1 10g A2-5 20 g B1 9g Polyacrylic acid thickening agent 1g Water 60g - - 40%
• Example 2 A1-2 10g A2-6 16 g B2 13g Polyacrylic acid thickening agent 1g Water 60g - - 40%
• Example 3 A1-3 10g A2-8 16 g B3 13g Polyacrylic acid thickening agent 1g Water 60g - - 40%
• Example 4 A1-4 10g A2-7 16 g B4 13g Carbomer 1g Water 60g - - 40%
• Example 5 A1-1 10g A2-8 16 g B4 13g Polyacrylamide 1g Water 60g - - 40%
• Example 6 A1-1 10g A2-5 9g B1 10 g Polyacrylic acid
• the water in the above table was deionized water.
• Example 1-3 The preparation process in Examples 1-3: The component A and component B in Table 2 were mixed, heated to 55-60°C, and fully stirred; the system was kept at a constant temperature, 40-50% of the component D and 90% of the component C were slowly added thereto while stirring, and the pH was regulated to 6.5-7. The above emulsion was homogenized, and was diluted with the balance amount of the component C and component D to obtain the defoaming agent product with corresponding solid content.
• Example 4-7 The preparation process in Examples 4-7: The component A and component B in Table 2 were mixed, heated to 60-70°C, and fully stirred; the system was kept at a constant temperature, 30-35% of the component D and 85% of the component C were slowly added thereto while stirring, and the pH was regulated to 6.5-7. The above emulsion was homogenized, and was diluted with the balance amount of the component C and component D to obtain the defoaming agent product with corresponding solid content.
• Example 8-9 The preparation process in Examples 8-9: The component A, component B and component E in Table 2 were mixed, heated to 50-80°C, and fully stirred; the system was kept at a constant temperature, 45-50% of the component D and 90% of the component C were slowly added thereto while stirring, and the pH was regulated to 6.5-7. The above emulsion was homogenized, and was diluted with the balance amount of the component C and component D to obtain the defoaming agent product with corresponding solid content.
• Example 10 The preparation process in Example 10: The component A, component B and component E in Table 2 were mixed, heated to 50-80°C, and fully stirred; the system was kept at a constant temperature, 30-40% of the component D and 85% of the component C were slowly added thereto while stirring, and the pH was regulated to 6.5-7. The above emulsion was homogenized, and was diluted with the balance amount of the component C and component D, and then the component F was added to obtain the defoaming agent product with corresponding solid content.
• the defoaming agents in comparative examples 1-14 were respectively prepared as per the formulae in Table 3. In each comparative example, the defoaming agent with corresponding solid content was prepared respectively using the process in Example 1 or Example 9.
• Table 3 Comparative example group Component A and use level Component B and use level Component C and use level Component D and use level Component E and use level Defoaming agent solid content Comparative example 1 A1-1 30 g - B1 9g Polyacrylic acid thickening agent 1 g Water 60 g 40% Comparative example 2 - A2-6 30 g B1 9g Polyacrylic acid thickening agent 1 g Water 60 g 40% Comparative example 3 - A-9 B1 9g Polyacrylic acid Water 60 g 40% 30 g thickening agent 1 g Comparative example 4 - A-13 30 g B19g Polyacrylic acid thickening agent 1 g Water 60 g 40% Comparative example 5 A1-1 10 g A-13 20 g B19g Polyacrylamide 1 g Water 60 g 40%
• Performance test of an organosilicone defoaming agent (1) Machine wash performance test in a liquid detergent The washing machine used in the test was a drum washing machine of Zanussi brand, model: ZWH6125, capacity: 7kg. Test method: 50 g of detergent available on the market, 0.1 g of the prepared orgnaosilicone emulsion and 20 kg of water were added to the washing machine, and then the program for cotton and linen was selected.
• the view window of the washing machine is marked with 5 scale values, respectively representing 0, 25%, 50%, 75% and 100% height of the view window. "0" is the start representing no foam, while "100%" represents full of foam. The foam height was recorded once every 5minutes, and was recorded at the time of stop.
• the compatibility and clarity of the defoaming agent in Examples 2, 4-5, 8 and 10 are close to or equivalent to the compatibility and clarity of the defoaming agent in Example 1.
• the compatibility and synergistic effect between the components A1 and A2 in a defoaming agent enable it to be closely bound with an organosilicon composition, not only have a better defoaming performance, but also improve the emulsion stability, and have more prominent advantages in compatibility and clarity.
• the effect is far better than that of the defoaming agent using only a single component A or using a combination that has a structure close to the structure of A1 and A2, but is not A1 or A2.

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